| Literature DB >> 34822203 |
Xiping Jiang1,2,3, Melinda Wojtkiewicz4, Chinmay Patwardhan5, Sydney Greer1,3, Yunfan Kong1, Mitchell Kuss1, Xi Huang6, Jun Liao5, Yongfeng Lu6, Andrew Dudley1,3, Rebekah L Gundry4, Matthias Fuchs7, Philipp Streubel8, Bin Duan1,2,9,10.
Abstract
Rotator cuff tendon injuries often occur at the tendon-to-bone interface (i.e., enthesis) area, with a high prevalence for the elderly population, but the underlying reason for this phenomenon is still unknown. The objective of this study is to identify the histological, molecular, and biomechanical alterations of the rotator cuff enthesis with maturation and aging in a mouse model. Four different age groups of mice (newborn, young, adult, and old) were studied. Striking variations of the entheses were observed between the newborn and other matured groups, with collagen content, proteoglycan deposition, collagen fiber dispersion was significantly higher in the newborn group. The compositional and histological features of young, adult, and old groups did not show significant differences, except having increased proteoglycan deposition and thinner collagen fibers at the insertion sites in the old group. Nanoindentation testing showed that the old group had a smaller compressive modulus at the insertion site when compared with other groups. However, tensile mechanical testing reported that the old group demonstrated a significantly higher failure stress when compared with the young and adult groups. The proteomics analysis detected dramatic differences in protein content between newborn and young groups but minor changes among young, adult, and old groups. These results demonstrated: (1) the significant alterations of the enthesis composition and structure occur from the newborn to the young time period; (2) the increased risk of rotator cuff tendon injuries in the elderly population is not solely because of old age alone in the rodent model.Entities:
Keywords: age; biomechanical properties; enthesis; nanoindentation; proteomics
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Year: 2021 PMID: 34822203 PMCID: PMC8959997 DOI: 10.1096/fj.202101484R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191